Dyke–Davidoff–Masson syndrome in a Nigerian

Philip B. Adebayo , Amnat Bakare , Modupe M. Bello , Opeyemi D. Olaewe , Kolawole W. Wahab
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引用次数: 9

Abstract

Dyke–Davidoff–Masson syndrome (DDMS) is a rare, but important cause of drug-resistant seizures. Dyke–Davidoff–Masson syndrome is a constellation of clinical features that consists of hemiparesis, seizure, facial asymmetry, and intellectual disability with distinct neuroimaging features. A 27-year-old lady presented to us with drug-resistant epilepsy, hemiparesis, and intellectual disability that necessitated her withdrawal from school. Her brain magnetic resonance imaging (MRI) showed cerebral hemiatrophy, calvarial thickening, and hyperpneumatization of the frontal sinuses consistent with DDMS. We discuss the diagnostic and therapeutic implications of DDMS and advocate early referral and evaluation of people with epilepsy in sub-Saharan African settings.

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尼日利亚人的Dyke-Davidoff-Masson综合症
Dyke-Davidoff-Masson综合征(DDMS)是一种罕见但重要的耐药性癫痫发作病因。Dyke-Davidoff-Masson综合征是一系列临床特征,包括偏瘫、癫痫发作、面部不对称和智力残疾,具有明显的神经影像学特征。一位27岁的女士向我们提出了抗药性癫痫,偏瘫和智力残疾,她必须从学校退学。她的脑磁共振成像(MRI)显示大脑半萎缩,颅骨增厚,额窦过度充气,与DDMS一致。我们讨论了DDMS的诊断和治疗意义,并提倡对撒哈拉以南非洲地区的癫痫患者进行早期转诊和评估。
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